原子转移自由基聚合
共聚物
高分子化学
丙烯酸
甲基丙烯酸
聚合
催化作用
自由基聚合
链式转移
聚合物
活性自由基聚合
可逆加成-断裂链转移聚合
反应性(心理学)
材料科学
化学
有机化学
医学
替代医学
病理
作者
Francesca Lorandi,Marco Fantin,Yi Wang,Abdirisak Ahmed Isse,Armando Gennaro,Krzysztof Matyjaszewski
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2020-04-27
卷期号:9 (5): 693-699
被引量:31
标识
DOI:10.1021/acsmacrolett.0c00246
摘要
The preparation of poly(acrylic acid) (PAA) with tailored architecture and morphology is important for the design of advanced polymer materials. Cu-catalyzed atom transfer radical polymerization (ATRP) of AA is challenging due to the tendency of dormant chains to undergo an intramolecular lactonization reaction with consequent loss of chain-end functionalities, as previously reported for ATRP of methacrylic acid (MAA). In addition, AA can coordinate to the Cu catalyst. Moreover, the lower ATRP reactivity of AA relative to MAA enhances side reactions during polymerizations. These issues were overcome by adjusting the composition of the catalytic system, the polymerization setup, and the initiator nature. AA conversion >70-80% was obtained in 5 h, producing PAA with Đ ≈1.4. Multifunctional water-soluble initiators provided PAA and PMAA with telechelic and star-shaped architectures. Block copolymers of MAA and AA confirmed the retention of chain-end functionalities during ATRPs.
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